Evidence map›Paper›PMID 23428900›Full record

ArticleInternational journal for parasitology2013

Deorphanization and target validation of cross-tick species conserved novel Amblyomma americanum tick saliva protein.

Albert Mulenga, Tae Kwon Kim, Adriana Mércia Guaratini Ibelli

Abstract read
In one paragraph

Article in International journal for parasitology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.6field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Article
  3. RecombinantPathogens (Basel, Switzerland) · 2024
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  5. Key molecules regulating the blood meals ofVeterinary research forum : an international quarterly journal · 2024
    Article
  6. Article
  7. Article
  8. The Impact of RNA Interference in Tick Research.Pathogens (Basel, Switzerland) · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Frontiers in immunology · 2020
    Article
  16. Novel and SelectiveVeterinary sciences · 2018
    Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Albert MulengaTexas A & M University AgriLife Research, Department of Entomology, 2475 TAMU, College Station, TX 77843, USA. a-mulenga@tamu.edu
Tae Kwon Kim
Adriana Mércia Guaratini Ibelli
Texas A&M University · US

Funding

Tick feeding regulation by orthologous tick saliva serine protease inhibitorsR01AI093858 · NIAID · TEXAS A&M UNIVERSITY · PI MULENGA, ALBERT · 2011 to 2014
$1.0M
Molecular Mechanisms Regulating Early Stage Tick FeedingR21AI081093 · NIAID · TEXAS A&M UNIVERSITY · PI MULENGA, ALBERT · 2011 to 2012
$404k
NIAID NIH HHS AI081093NIAID NIH HHS R01 AI093858NIAID NIH HHS R21 AI081093
6 · The paper itself

Abstract

We previously identified a cross-tick species conserved tick feeding stimuli responsive Amblyomma americanum (Aam) AV422 gene. This study demonstrates that AamAV422 belongs to a novel group of arthropod proteins that is characterized by 14 cysteine amino acid residues: C(23)-X7/9-C(33)-X23/24-C(58)-X8-C(67)-X7-C(75)-X23-C(99)-X15-C(115)-X10-C(126)-X24/25/33-C(150)C(151)-X7-C(159)-X8-C(168)-X23/24-C(192)-X9/10-C(202) predicted to form seven disulfide bonds. We show that AamAV422 protein is a ubiquitously expressed protein that is injected into the host within the first 24h of the tick attaching onto the host as revealed by Western blotting analyses of recombinant (r)AamAV422, tick saliva and dissected tick organ protein extracts using antibodies to 24 and 48 h tick saliva proteins. Native AamAV422 is apparently involved with mediating tick anti-hemostasis and anti-complement functions in that rAamAV422 delayed plasma clotting time in a dose responsive manner by up to ≈ 160 s, prevented platelet aggregation by up to ≈ 16% and caused ≈ 24% reduction in production of terminal complement complexes. Target validation analysis revealed that rAamAV422 is a potential candidate for a cocktail or multivalent tick vaccine preparation in that RNA interference (RNAi)-mediated silencing of AamAV422 mRNA caused a statistically significant (≈ 44%) reduction in tick engorgement weights, which is proxy for amounts of ingested blood. We speculate that AamAV422 is a potential target antigen for development of the highly desired universal tick vaccine in that consistent with high conservation among ticks, antibodies to 24h Ixodes scapularis tick saliva proteins specifically bound rAamAV422. We discuss data in this study in the context of advancing the biology of tick feeding physiology and discovery of potential target antigens for tick vaccine development.

Indexed as

Conserved SequenceAnimalsBlood CoagulationComplement System ProteinsFeeding BehaviorIxodidaeMolecular Sequence DataPlatelet AggregationRabbitsSalivary Proteins and PeptidesSequence Analysis, DNAComplement System ProteinsSalivary Proteins and Peptides

Identifiers

PMID23428900
PMCPMC4058329
OpenAlexW2022370671

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.